| Literature DB >> 31025566 |
Pengfei Yang1, Weiyan Xu1, Rongchao Wang1, Min Zhang1, Chunsong Xie1, Xiaofei Zeng1, Min Wang1.
Abstract
An efficient and facile method to synthesize valuable disubstituted 2-aryl indoles and benzofurans in good yields has been demonstrated, based on a tert-butoxide-mediated condensation reaction involving a vinyl sulfoxide intermediate. Products are obtained from N- or O-benzyl benzaldehydes using dimethyl sulfoxide as a carbon source. The methodology features a wide functional group tolerance and transition metal-free environment. Preliminary mechanistic studies suggest that the reaction involves a tandem aldol reaction/Michael addition/dehydrosulfenylation/isomerization sequence through an ionic protocol.Entities:
Year: 2019 PMID: 31025566 DOI: 10.1021/acs.orglett.9b01093
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005